31 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SYNTHES 4.0 AND 5.0 MM LOCKING SCREWS
FDA 510(k)
FDA Class 2
·Orthopedic
4.0MM TI LOCKING SCREW W/T25 STARDRIVE 34MM F/IM NAILS-STER
FDA Adverse Event
Injury
·SYNTHES USA·Product code HSB·September 20, 2013
4.0MM TI LOCKING SCREW W/T25 STARDRIVE 44MM F/IM NAILS-STER
FDA Adverse Event
Injury
·SYNTHES USA·Product code HSB·September 20, 2013
SCREW,FIXATION,BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HWC·May 18, 2015
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·August 27, 2015
5.0MM TI LOCKING SCREW W/T25 STARDRIVE 56MM FOR IM NAILS
FDA Adverse Event
Injury
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·April 11, 2018
Custom Procedure Kit
FDA UDI
MEDIVATORS INC.·40677964001503·The ENDO CARRY-ON Procedure Kit contains all of...
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040043639·Forcep Extracting #88L SG
THORATEC® PVAD™, LVAD ELECTRICAL EXTENSION LEAD 7FT
FDA UDI
Thoratec Corporation·00813024012672·
EXPRESS VASCULAR LD PREMOUNTED STENT SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC·Product code NIO·April 8, 2005
Truelink
FDA UDI
Statcorp Medical·10841522124136·6.5FT GRAY TWIN HOSE W/ TWIN TUBE CONNECTORS 1EA
SINGLE SIZE TENDON SPACER
FDA 510(k)
FDA Class 2
·Orthopedic
SPIRAL RADIUS RODDING SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
6000089-2006-00036
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC·February 13, 2006
6000089-2006-02481
FDA Adverse Event
Injury
·Product code LIT·November 21, 2006
6000089-1999-00116
FDA Adverse Event
Injury
·December 29, 1999
6000089-1999-00113
FDA Adverse Event
Malfunction
·December 21, 1999
6000089-1999-00115
FDA Adverse Event
Injury
·December 29, 1999
6000089-1999-00114
FDA Adverse Event
Injury
·December 29, 1999
6000089-1999-00117
FDA Adverse Event
Injury
·December 29, 1999